T-cell subsets and soluble factors of immune system activation are inc
reasingly used as biologic markers of disease and predictors of diseas
e progression. For example, changes in CD4 cells and CD4:CD8 ratio, sI
L-2R, B2M, neopterin, and IgA have been used in predicting AIDS onset
and progression. We examined the temporal variability of T-cell subset
s, monocytes, natural killer cells, B cells, immunoglobulins, soluble
interleukin-2 receptor (sIL-2R), neopterin, and beta-2 microglobulin (
B2M) among 135 adults tested at two time points similar to 3 months ap
art. The purpose of the study was twofold: (1) to assess the stability
of these measures at two points in time, and (2) to investigate which
parameters tend to track together over time, i.e., show significant l
ongitudinal correlation. Mean population values for these immunologic
parameters remained remarkably stable over the 3-month period. However
, individual subjects exhibited significant temporal variability for m
any parameters. Unlike observations in patients with AIDS, changes in
immunoglobulins and other soluble factors were not significantly corre
lated with changes in cellular subsets over the same period. However,
change in B2M was correlated with change in neopterin (r = .35, P less
than or equal to .0001), and change in IgA was correlated with change
s in IgG and IgM (r = .44, r = .54, P less than or equal to .001 for b
oth). Characterizing this temporal variability in a healthy population
provides important information for researchers applying these tests i
n clinical and epidemiological studies. (C) 1997 Wiley-Liss, Inc.